Amlodipine Besylate
Product Images NDC 76413-141

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate (NDC 76413-141). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Central Texas Community Health Centers, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Structured Formula For Amlodipine (33b920c2 99ae 4d3e Ab21 0d349d0e64ed 01)

Chemical structure of Amlodipine Besylate, showing its molecular components including a benzene ring with chlorine, various functional groups such as esters, amines, and ethers arranged in a complex structure.*

FDA Label Image

Structured Formula For Amlodipine (33b920c2 99ae 4d3e Ab21 0d349d0e64ed 02)

A Kaplan-Meier curve showing event rate over time (months) comparing Amlodipine and Placebo groups. The graph includes hazard ratio, p-value, and 95% confidence interval, with numbers at risk listed below the time axis.*

FDA Label Image

Structured Formula For Amlodipine (33b920c2 99ae 4d3e Ab21 0d349d0e64ed 03)

A forest plot showing hazard ratios with 95% confidence intervals comparing Amlodipine versus placebo across various patient subgroups including overall, age, gender, baseline sitting systolic blood pressure, baseline vessel disease, baseline vessels with stenosis, and PCI-stent strata. The horizontal axis displays hazard ratios from 0 to 2, with a reference line at 1 indicating no difference between treatments.*

FDA Label Image

Principal Display Panel (5 MG Tablet Bottle Label)

A prescription label for Amlodipine Besylate 5 mg, quantity 30 tablets, from Central Texas Community Health Centers. The label includes dosage instructions in English and Spanish, a batch number (123456), lot number (123456), expiration date (1/1/01), and the NDC 76413-141-30. It is issued by Austin's Health & Human Services Dept.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.